{"orpha":715694,"name":"Infant-type hemispheric glioma NTRK-altered","type":"Etiological subtype","group":"Subtype of disorder","status":"active","flags":[],"synonyms":[],"definition":null,"note":null,"url":"https://raremap.alftech.space/d/ORPHA-715694/","orphanet_url":"https://www.orpha.net/en/disease/detail/715694","names":{"fr":{"name":"Gliome hémisphérique infantile NTRK-altéré"},"de":{"name":"Hemisphärisches Gliom vom infantilen Typ mit NTRK-Alteration"},"es":{"name":"Glioma hemisférico de tipo infantil con alteración de NTRK"},"it":{"name":"Glioma emisferico tipo infantile con alterazione di NTRK"},"nl":{"name":"Infantiel hemisferisch glioom NTRK-gewijzigd"},"pt":{"name":"Infant-type hemispheric glioma NTRK-altered"},"pl":{"name":"Glejak półkulisty typu niemowlęcego ze zmianą NTRK"},"cs":{"name":"Infant-type hemispheric glioma NTRK-altered"}},"xrefs":[],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":250908,"name":"Rare neoplastic disease"},"parents":[{"orpha":695136,"name":"Infant-type hemispheric glioma","classifications":[181,202]}],"children":[],"genes":[{"symbol":"NTRK1","name":"neurotrophic receptor tyrosine kinase 1","gene_type":"gene with protein product","association":"Part of a fusion gene in","status":"Assessed","source":"36601394[PMID]_31554817[PMID]_35034013[PMID]","hgnc":"8031","ensembl":"ENSG00000198400","omim":"191315","loci":["1q23.1"]},{"symbol":"NTRK2","name":"neurotrophic receptor tyrosine kinase 2","gene_type":"gene with protein product","association":"Part of a fusion gene in","status":"Assessed","source":"36601394[PMID]_31554817[PMID]_35034013[PMID]","hgnc":"8032","ensembl":"ENSG00000148053","omim":"600456","loci":["9q21.33"]},{"symbol":"NTRK3","name":"neurotrophic receptor tyrosine kinase 3","gene_type":"gene with protein product","association":"Part of a fusion gene in","status":"Assessed","source":"36601394[PMID]_31554817[PMID]_35034013[PMID]","hgnc":"8033","ensembl":"ENSG00000140538","omim":"191316","loci":["15q25.3"]}],"genes_via_subtypes":[],"inheritance":["Not applicable"],"onset":[],"prevalence":[],"phenotypes":null}